Evolution of the caregiving experience in the initial 2 years following stroke.

Relationships between stroke survivor and family caregiver factors and the caregiver's health-related quality of life (HRQL) and overall quality of life (QoL) were examined in 97 dyads during the first and second years after stroke. Compared to age- and sex-matched population norms, caregivers scored significantly lower on the mental subscales of HRQL, and differences were greater for women than for men. Caregiver characteristics (older age, less burden, and fewer physical symptoms) were associated with better HRQL (mental summary scale) in the first year, with similar findings in the second year. Moderate stroke survivor physical impairment and caregiver characteristics (younger age and better HRQL) were associated with better QoL in the first year. During the second year poorer caregiver physical and mental health and caring for a stroke survivor with communication difficulties were associated with diminished QoL.

[1]  Nancy E. Avis,et al.  Distinguishing between quality of life and health status in quality of life research: A meta-analysis , 1999, Quality of Life Research.

[2]  P. Jacobsen,et al.  The Caregiver Quality of Life Index–Cancer (CQOLC) scale: development and validation of an instrument to measure quality of life of the family caregiver of patients with cancer , 2004, Quality of Life Research.

[3]  J. Ware SF-36 health survey: Manual and interpretation guide , 2003 .

[4]  S. Wood-Dauphinée,et al.  Activity, participation, and quality of life 6 months poststroke. , 2002, Archives of physical medicine and rehabilitation.

[5]  P. Duncan,et al.  Caregiving experiences after stroke. , 2001, Nursing research.

[6]  John E. Ware,et al.  SF-36 Health Survey Update , 2000, Spine.

[7]  Jacques P. Brown,et al.  Canadian normative data for the SF-36 health survey. Canadian Multicentre Osteoporosis Study Research Group. , 2000, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.

[8]  R. Schulz,et al.  Gender differences in psychiatric morbidity among family caregivers: a review and analysis. , 2000, The Gerontologist.

[9]  P. Roderick,et al.  The impact of stroke on informal carers: a literature review. , 1999, Social science & medicine.

[10]  C. Bugge,et al.  Stroke patients' informal caregivers. Patient, caregiver, and service factors that affect caregiver strain. , 1999, Stroke.

[11]  W. Haley,et al.  Family caregiving for patients with stroke. Review and analysis. , 1999, Stroke.

[12]  P. Knapp,et al.  Disagreement in patient and carer assessment of functional abilities after stroke. , 1999, Stroke.

[13]  J. Hanley,et al.  Proxy use of the Canadian SF-36 in rating health status of the disabled elderly. , 1998, Journal of clinical epidemiology.

[14]  C. Warlow,et al.  A quantitative study of the emotional outcome of people caring for stroke survivors. , 1998, Stroke.

[15]  P. Kind,et al.  Measuring health status in British patients with rheumatoid arthritis: reliability, validity and responsiveness of the short form 36-item health survey (SF-36). , 1998, British journal of rheumatology.

[16]  M. Strauss,et al.  Differences in the perceived well-being of wives and husbands caring for persons with Alzheimer's disease. , 1998, The Gerontologist.

[17]  S. Black,et al.  The Sunnybrook Stroke Study: a prospective study of depressive symptoms and functional outcome. , 1998, Stroke.

[18]  H. C. Hanger,et al.  What do patients and their carers want to know about stroke? A two-year follow-up study , 1998, Clinical rehabilitation.

[19]  K. Goode,et al.  Gender roles and caregiving stress: An examination of subjective appraisals of specific primary stressors in Alzheimer's caregivers , 1997 .

[20]  R. Langton-Hewer,et al.  Identification of stroke carers 'at risk': a preliminary study of the predictors of carers' psychological well-being at one year post stroke , 1996 .

[21]  M. Seltzer,et al.  The transitions of caregiving: subjective and objective definitions. , 1996, The Gerontologist.

[22]  T. Mulder,et al.  Long‐term outcome after stroke: a disability‐orientated approach , 1996, International journal of rehabilitation research. Internationale Zeitschrift fur Rehabilitationsforschung. Revue internationale de recherches de readaptation.

[23]  H van Veenendaal,et al.  Educational needs of stroke survivors and their family members, as perceived by themselves and by health professionals. , 1996, Patient education and counseling.

[24]  B. Mount,et al.  Defining quality of life. , 1996, European journal of cancer.

[25]  Alison T. O'Brien,et al.  Psychiatric and physical morbidity effects of dementia caregiving: prevalence, correlates, and causes. , 1995, The Gerontologist.

[26]  C. Anderson,et al.  A population-based assessment of the impact and burden of caregiving for long-term stroke survivors. , 1995, Stroke.

[27]  S. Saxena,et al.  The World Health Organization Quality of Life assessment (WHOQOL): position paper from the World Health Organization. , 1995, Social science & medicine.

[28]  A. Gross,et al.  Caregivers of Alzheimer's disease and stroke patients: immunological and psychological considerations. , 1994, The Gerontologist.

[29]  C. Sherbourne,et al.  The MOS 36-item Short-Form Health Survey (SF-36): III. Tests of data quality, scaling assumptions, and reliability across diverse patient groups. , 1994 .

[30]  John E. Ware,et al.  SF-36 physical and mental health summary scales : a user's manual , 1994 .

[31]  B. Miller,et al.  Gender differences in caregiving: fact or artifact? , 1992, The Gerontologist.

[32]  J. E. Brazier,et al.  Validating the SF-36 health survey questionnaire: new outcome measure for primary care. , 1992, BMJ.

[33]  C. Sherbourne,et al.  The MOS 36-Item Short-Form Health Survey (SF-36) , 1992 .

[34]  Robert Anderson,et al.  The Aftermath of Stroke : Index , 1992 .

[35]  S. Gauthier,et al.  The psychological and physical health of family members caring for an elderly person with dementia. , 1992, Journal of clinical epidemiology.

[36]  J. French,et al.  Long-term outcome for patients and carers following hospital admission for stroke. , 1991, Age and ageing.

[37]  H. Young,et al.  Burden: a review of measures used among caregivers of individuals with dementia. , 1991, The Gerontologist.

[38]  R. Schulz,et al.  Family Caregiving in Chronic Illness , 1990 .

[39]  B. Norrving,et al.  Outcome after stroke in patients discharged to independent living. , 1990, Stroke.

[40]  G. Guyatt,et al.  Measuring quality of life in cardiac spouses. , 1990, Journal of clinical epidemiology.

[41]  B Cooper,et al.  Improving the sensitivity of the Barthel Index for stroke rehabilitation. , 1989, Journal of clinical epidemiology.

[42]  R. Schulz,et al.  A longitudinal study of the psychosocial impact of stroke on primary support persons. , 1988, Psychology and aging.

[43]  B. Pentland,et al.  An inter-rater reliability study of the Barthel Index , 1988 .

[44]  R. Schulz,et al.  Post-stroke depression in primary support persons: predicting those at risk. , 1988, Journal of consulting and clinical psychology.

[45]  T. Carnwath,et al.  Psychiatric morbidity among spouses of patients with stroke. , 1987, British medical journal.

[46]  R. Anderson The unremitting burden on carers. , 1987, British medical journal.

[47]  R. Fletcher,et al.  Families of Elderly Stroke Patients , 1986, Journal of the American Geriatrics Society.

[48]  D. Wade,et al.  Effects of living with and looking after survivors of a stroke. , 1986, British medical journal.

[49]  S. Zarit,et al.  Subjective burden of husbands and wives as caregivers: a longitudinal study. , 1986, The Gerontologist.

[50]  C. Pratt,et al.  Family Caregivers and Dementia , 1986 .

[51]  C. Sherbourne,et al.  Effects of cost sharing on seeking care for serious and minor symptoms. Results of a randomized controlled trial. , 1986, Annals of internal medicine.

[52]  S. Zarit,et al.  Relatives of the impaired elderly: correlates of feelings of burden. , 1980, The Gerontologist.

[53]  D. Goldberg,et al.  A scaled version of the General Health Questionnaire , 1979, Psychological Medicine.

[54]  Granger Cv,et al.  Stroke rehabilitation: analysis of repeated Barthel index measures. , 1979, Archives of physical medicine and rehabilitation.

[55]  J. C. Flanagan A research approach to improving our quality of life. , 1978 .

[56]  Lu Ann Aday,et al.  Development of indices of access to medical care , 1975 .

[57]  M. Hamilton,et al.  Assessment of the severity of primary depressive illness: Wakefield self-assessment depression inventory , 1971, Psychological Medicine.